Possible Impact of Cytomegalovirus-Specific CD8+ T Cells on Immune Reconstitution and Conversion to Complete Donor Chimerism after Allogeneic Stem Cell Transplantation

被引:23
|
作者
Ogonek, Justyna [1 ]
Varanasi, Pavankumar [1 ,2 ]
Luther, Susanne [1 ]
Schweier, Patrick [1 ]
Kuehnau, Wolfgang [3 ]
Goehring, Gudrun [3 ]
Dammann, Elke [1 ]
Stadler, Michael [1 ]
Ganser, Arnold [1 ]
Borchers, Sylvia [4 ]
Koehl, Ulrike [5 ]
Weissinger, Eva M. [1 ,2 ]
Hambach, Lothar [1 ]
机构
[1] Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, D-30625 Hannover, Germany
[2] German Ctr Infect Res DZIF, Partner Site Hannover Braunschweig, Hannover, Germany
[3] Hannover Med Sch, Dept Human Genet, Hannover, Germany
[4] RHEACELL GmbH & Co KG, Heidelberg, Germany
[5] Hannover Med Sch, Inst Cellular Therapeut, Hannover, Germany
关键词
Chimerism; T cell reconstitution; CMV-specific T cells; Antithymocyte globulin; ACUTE MYELOID-LEUKEMIA; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; RELAPSE RISK EVIDENCE; REDUCED-INTENSITY; CONDITIONING REGIMEN; MIXED CHIMERISM; MYELODYSPLASTIC SYNDROME; ANTITHYMOCYTE GLOBULIN; ENDOTHELIAL-CELLS;
D O I
10.1016/j.bbmt.2017.03.027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Complete donor chimerism is strongly associated with complete remission after allogeneic stem cell transplantation (allo-SCT) in patients with hematologic malignancies. Donor-derived allo-immune responses eliminate the residual host hematopoiesis and thereby mediate the conversion to complete donor chimerism. Recently, cytomegalovirus (CMV) reactivation was described to enhance overall T cell reconstitution, to increase graft-versus-host disease incidence, and to reduce the leukemia relapse risk. However, the link between CMV and allo-immune responses is still unclear. Here, we studied the relationship between CMV-specific immunity, overall T cell reconstitution, and residual host chimerism in 106 CMV-seropositive patients transplanted after reduced-intensity conditioning including antithymocyte globulin. In accordance with previous reports, the recovery of CMV-specific cytotoxic T cells (CMV-CTLs) was more frequent in CMV-seropositive recipients (R) transplanted from CMV-seropositive than from seronegative donors (D). However, once CMV-CTLs were detectable, the reconstitution of CMV-specific CfLs was comparable in CMV R+/D- and R+/D+ patients. CD3(+) and CD8(+) T cell reconstitution was significantly faster in patients with CMV-CTLs than in patients without CMV-CTLs both in the CMV R+/D- and R+/D+ setting. Moreover, CMV-CTL numbers correlated with CD3(+) and CD8(+)T cell numbers in both settings. Finally, presence of CMV-CTLs was associated with low host chimerism levels 3 months after allo-SCT. In conclusion, our data provide a first indication that CMV-CTLs in CMV-seropositive patients might trigger the reconstitution of T cells and alto-immune responses reflected by the conversion to complete donor chimerism. (C) 2017 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1046 / 1053
页数:8
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